"Genetic Services Laboratory, University of Chicago"[submitter] AND "R - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1166723	NM_017763.6(RNF43):c.2261G>C (p.Gly754Ala)	RNF43 (G627A +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 1111196	NM_017763.6(RNF43):c.674G>A (p.Arg225His)	RNF43 (R225H +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GLikely benign
Select item 1165411	NM_017763.6(RNF43):c.576G>A (p.Pro192=)	RNF43	Single nucleotide variant (synonymous variant)	RNF43-related condition +2 more	GBenign/Likely benign
Select item 1338203	NM_017763.6(RNF43):c.407C>T (p.Ala136Val)	RNF43 (A136V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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